Catalog No.
Product Name
Application
Product Information
Citations
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Endogenous Metabolite
D-Ribofuranose serves as an endogenous metabolite that plays a crucial role in cellular metabolism. It is primarily involved in the synthesis of nucleotides and nucleic acids. Research applications include studies related to Ribose 5 Phosphate Isomerase Deficiency and Medium Chain Acyl-CoA Dehydrogenase Deficiency, providing insights into metabolic pathways and associated disorders. -
Precursor of HMG-CoA
Acetoacetyl-CoA is a key precursor of HMG-CoA in the mevalonate pathway, playing a crucial role in cholesterol biosynthesis. It is generated through the action of acetoacetyl-CoA thiolase, which catalyzes the condensation of two acetyl-CoA molecules. Additionally, acetoacetyl-CoA serves as an important intermediate in the metabolism of fatty acids, contributing to both their breakdown and synthesis. This compound is valuable for research in lipid metabolism and the regulation of cholesterol levels. -
Fungal Metabolite
Gliorosein is a fungal metabolite derived from Gliocladium, functioning primarily as an isomeric variant of quinol. It exhibits distinct ultraviolet absorption characteristics, differentiating it from related compounds. This unique profile makes Gliorosein valuable for biological research applications, particularly in the study of fungal metabolism and ecological interactions. -
Endogenous Metabolite
Endopeptidase-IN-1 is a potent inhibitor of endopeptidase activity, targeting endogenous metabolites to regulate proteolytic processes. Its biological activity is crucial for research focused on protein processing, cellular signaling pathways, and the modulation of metabolic diseases. This compound is a valuable tool for investigating the role of endopeptidases in physiological and pathological conditions. -
Endogenous Metabolite
YM-75440 is an orally active inhibitor of squalene synthase, a key enzyme in the cholesterol biosynthesis pathway. This compound demonstrates significant biological activity in modulating lipid metabolism, making it useful for research on metabolic disorders and cardiovascular diseases. Its ability to inhibit squalene synthesis positions YM-75440 as a valuable tool for studying cholesterol-related pathways and potential therapeutic interventions. -
Endogenous Metabolite
Wofapyrin, a derivative of Rheumopyrin, primarily acts as an antipyretic and anti-inflammatory agent. This compound has demonstrated significant biological activity in reducing lesion volume, positioning it as a valuable reagent in studies focused on inflammation and fever regulation. Its application is pertinent for researchers investigating metabolic pathways and therapeutic interventions in inflammatory conditions. -
Endogenous Metabolite
alpha-RA-F (α-RA-F) is an endogenous metabolite that promotes collagen synthesis while reducing the expression levels of matrix metalloproteinases (MMPs). Its ability to enhance collagen production in human fibroblasts without cytotoxicity makes α-RA-F a valuable tool for research in tissue regeneration and skin health. This compound holds significant potential for applications in both pharmaceutical and cosmetic industries, particularly in the regulation of collagen dynamics and extracellular matrix remodeling. -
Endogenous Metabolite
R-(-)-Phencynonate hydrochloride is a muscarinic receptor antagonist that exhibits anticholinergic activity. This compound serves as a significant endogenous metabolite, making it integral for investigations related to its concentration in human plasma within medical research contexts. R-(-)-Phencynonate has been effectively analyzed using high-performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS), demonstrating excellent specificity and linearity for precise quantification. -
Endogenous Metabolite
1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE is a phospholipid featuring stearic acid at the sn-1 position and 15(S)-HETE at the sn-2 position. This compound is generated through the oxidation of 1-stearoyl-2-arachidonoyl-sn-glycero-3-PE by the enzyme 15-lipoxygenase in activated human peripheral mononuclear cells. 1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE serves as an endogenous metabolite, providing valuable insights into lipid metabolism and cell signaling pathways in various biological research applications. -
Endogenous Metabolite
ts-SA is a potent carbonic anhydrase (CA) inhibitor that demonstrates inhibitory activity against seven human CA homologues. It effectively binds to the Zn(II) ion in the enzyme's active site in its deprotonated form, with its organic structure extending into the enzyme cavity, facilitating interactions with amino acid residues and water molecules. With low nanomolar inhibitory activity, ts-SA serves as a multi-target CA inhibitor, making it valuable for research applications in enzymatic regulation and metabolic studies. -
Endogenous Metabolite
DY3002 is a highly selective and potent EGFR inhibitor specifically designed to target T790M-mutated variants associated with non-small cell lung cancer. This compound demonstrates a remarkable inhibitory effect on EGFR T790M mutants with an IC50 of 0.71 nM, while exhibiting significantly reduced activity against wild-type EGFR (IC50 = 448.7 nM). In cellular assays, DY3002 shows an IC50 of 0.037 μM against H1975 cells, indicating enhanced biological efficacy. Additionally, DY3002 maintains an extraordinary selectivity index (SI = 632.0) and does not induce hyperglycemia, making it a promising candidate for further research in overcoming drug resistance in cancer therapy. -
Endogenous Metabolite
Ro 31-1118 Free Base is an endogenous metabolite that exhibits weak antihypertensive activity. It has been shown to reduce heart rates and blood pressure following exercise at various doses, demonstrating linear pharmacokinetics within the 10-80 mg range. Notably, Ro 31-1118 does not significantly affect diastolic blood pressure and shows minimal adverse effects, making it a valuable compound for studies related to cardiovascular function and blood pressure regulation. -
Endogenous Metabolite
1,3-Dioleoyl-2-lauroyl glycerol is an endogenous metabolite recognized for its role in the triglyceride composition of human milk. This compound can be analyzed using liquid chromatography-mass spectrometry, facilitating targeted studies of lipid metabolism and nutritional research. Its characterization contributes to the understanding of dietary fats and their influence on human health. -
Fungal Metabolite
Burnettramic acid A aglycone is a fungal metabolite derived from Aspergillus burnettii, exhibiting potential antimicrobial properties. This compound may play a significant role in research focused on antifungal activity and the exploration of secondary metabolites in fungi. Its unique chemical structure and biological functions make it a valuable reagent for studies in microbiology and natural product chemistry. -
Endogenous Metabolite
11β-13,14-Dihydro-15-keto Prostaglandin F2α is an endogenous metabolite that serves as a derivative of 13,14-Dihydro-15-keto PGF2α. This compound plays a significant role in various biological processes, particularly in pregnancy-related research. Its biological activity may facilitate the investigation of prostaglandin pathways and their implications in reproductive health and pregnancy maintenance. -
Endogenous Metabolite
MAO-B-IN-35 is a potent, selective, reversible inhibitor of monoamine oxidase B (MAO-B). Demonstrating strong inhibitory activity, this compound has significant potential for research applications related to neurodegenerative disorders and the modulation of monoamine neurotransmitter levels. Its design allows for efficient synthesis and superior physicochemical properties, making it a valuable tool for studying MAO-B's role in various biological processes. -
Endogenous Metabolite
Pyrimidine-indole hybrid is an endogenous metabolite that functions primarily as an antagonist of the Hedgehog signaling pathway through the destabilization of microtubules. This compound demonstrates significant biological activity by inhibiting ciliogenesis and disrupting the stable form of α-tubulin. Its unique mechanism of action has been validated in in vitro cell studies and in zebrafish embryo models, making it a valuable tool for investigating microtubule dynamics and related signaling processes. -
Endogenous Metabolite
5'-Guanidinonaltrindole TFA is a selective antagonist of the kappa-opioid receptor, demonstrating significant opioid antagonist activity. It exhibits an antagonistic potency five times greater than that of norbinatorphimine in smooth muscle preparations, with a selectivity ratio exceeding 500-fold. Binding and functional studies reveal pA(2) values aligning with the smooth muscle data, indicating its effectiveness. This compound serves as a valuable pharmacological tool for investigating the role of kappa-opioid receptors in opioid research. -
Endogenous Metabolite
Dipotassium glucose-6-phosphate (D-Glucose-6-phosphate dipotassium salt dihydrate) is a phosphorylated sugar that targets endogenous metabolic pathways. As a key intermediate in carbohydrate metabolism, it plays a crucial role in glycolysis and gluconeogenesis. This compound is widely used in biochemical and physiological studies to investigate metabolic processes and enzyme activity related to glucose metabolism. -
Endogenous Metabolite
ML-7 is a myosin light chain kinase inhibitor that primarily targets the regulation of superoxide anion (O2(-)) release in human neutrophils. This compound effectively inhibits extracellular O2(-) release from stimulated cells while leaving intracellular O2(-) production unaffected. Additionally, ML-7 has been shown to modulate neutrophil activity independently of myosin light chain kinase and offers protective effects on cardiac function during ischemia/reperfusion injury. Its unique properties make it valuable for research in inflammation and cardiac protection mechanisms. -
Endogenous Metabolite
Nafenopin is an endogenous metabolite that acts as a peroxidase proliferator, demonstrating liver tumor-promoting activity. This compound is recognized for its role in managing hyperlipoproteinemia and inducing oxidative stress in vivo, particularly in hepatic tissue. Nafenopin's unique mechanisms of action differentiate it from other non-genotoxic carcinogens, making it a valuable tool for research related to liver pathology and metabolic disorders. -
Endogenous Metabolite
Cellobiosan is an anhydrosugar derived from the combustion of biomass. As an endogenous metabolite, it plays a significant role in various biological processes, including energy metabolism and carbohydrate digestion. Cellobiosan is utilized in research applications focusing on metabolic pathways, the environmental impact of biomass burning, and the study of carbohydrate-derived compounds. -
Endogenous Metabolite
2,4-D methyl ester is an endogenous metabolite that serves as a biostimulant, promoting the accumulation of key nutritional and medicinal components. This compound has been shown to enhance the production of bioactive constituents in Cordyceps militaris, exhibiting an inductive effect that is concentration-dependent. Research applications include improving the fruit quality of Cordyceps militaris, making 2,4-D methyl ester a valuable tool for enhancing natural product yields in various biological studies. -
Endogenous Metabolite
04:1 Coenzyme A trisodium is a specific form of coenzyme A (CoA) characterized by a four-carbon acyl chain with one double bond. This reagent plays a critical role in various biochemical pathways, facilitating the transfer of acyl groups and participating in lipid metabolism. It is essential for studying metabolic processes, enzymatic reactions, and cellular signaling mechanisms involving acyl-CoA derivatives. -
Endogenous Metabolite
Xanthosine dihydrate is a nucleoside that serves as an endogenous metabolite, derived from xanthine and ribose. It has been shown to enhance the population of mammary stem cells and promote milk production in livestock such as cattle and goats. This compound is valuable for research in metabolic regulation and agricultural biotechnology. -
Endogenous Metabolite
Monononadecanoin is an endogenous metabolite known for its anti-inflammatory and antioxidant properties. This lipid compound is utilized in various research applications related to skin moisturization and repair, as well as flavor enhancement and preservation in food products. Its biological activities make it a valuable tool in studying skin health and food science. -
Endogenous Metabolite
Amino acid arylamidase, derived from hog kidney, is a metalloprotease that specifically hydrolyzes proteins or peptides with free α-amino or α-imino groups. This enzyme plays a significant role in amino acid metabolism and protein digestion. Its activity can be inhibited through N-terminal acetylation, making it a valuable tool in studies related to hepatic diseases, biliary disorders, and heart failure research. -
Endogenous Metabolite
2-(1-Hydroxypentyl)benzoic acid is an endogenous metabolite with potential therapeutic implications in the treatment of acute ischemic stroke (AIS). This compound may exert neuroprotective effects, making it a valuable candidate for research aimed at understanding stroke pathophysiology and developing novel therapeutic strategies. Its role in metabolic pathways and cellular signaling may provide insights into neuroprotection and recovery processes after ischemic events. -
Endogenous Metabolite
D-Glyceric acid calcium hydrate is an endogenous metabolite primarily involved in metabolic processes. It serves as a valuable research tool for studying primary hyperoxaluria type I and glutaric acidemia type 2. Its biological significance makes it useful in exploring metabolic disorders and related conditions. -
Endogenous Metabolite
1,2-Dioleoyl-3-α-linolenoyl-rac-glycerol is a triglyceride that serves as an endogenous metabolite, primarily studied for its role in lipid metabolism within the bumblebee fat body. Analytical techniques, including chromatography, have identified variations in fatty acid composition and triglyceride isomer distribution among different bumblebee species. This compound is valuable for research focused on insect physiology, lipid biochemistry, and comparative metabolomics. -
Herbicide
4-Chloropinselin is a chlorine-substituted xanthone that serves as an effective herbicide. This compound exhibits significant phytotoxicity, effectively inhibiting the growth of various weeds, including field sowthistle. Additionally, 4-Chloropinselin demonstrates antimicrobial properties, making it valuable for research in agricultural and microbiological applications. Its role as a biosynthetic precursor or degradation product of chloromonilicin further highlights its relevance in studying herbicidal mechanisms and microbial interactions. -
Auxin Herbicide
Fluroxypyr is an auxin herbicide that targets the plant auxin signaling pathway to effectively control both annual and perennial weeds. It works by inducing auxin overdose, leading to elevated endogenous auxin concentrations that disrupt auxin homeostasis and interact with other hormonal pathways in plant tissues. Fluroxypyr is widely used in agricultural research to study plant growth regulation and herbicide resistance mechanisms. -
Herbicide
Picloram is a synthetic auxin herbicide that targets growth regulation pathways in plants. It effectively controls a variety of dicotyledonous weeds by disrupting their normal growth processes. Picloram is commonly utilized in agricultural and environmental management applications to maintain crop health and improve land usability. Its selective herbicidal properties make it valuable for research on plant physiology and herbicide resistance. -
Bleaching Herbicide
Norflurazon is a bleaching herbicide that primarily targets phytoene desaturase, inhibiting carotenoid biosynthesis. This mechanism leads to the disruption of chlorophyll production in plants, resulting in bleaching and subsequent plant growth inhibition. Norflurazon is widely used in agricultural research to study herbicide resistance, plant physiology, and the effects of carotenoid depletion on plant metabolism. -
PROTOX Inhibitor
Acifluorfen is a protoporphyrinogen oxidase (PROTOX) inhibitor primarily utilized as a herbicide. It effectively promotes the accumulation of protoporphyrin IX (PPIX), leading to significant photooxidative damage in sensitive plant species. Additionally, Acifluorfen has been shown to induce tumors in rodent liver models, making it relevant for research applications focused on oxidative stress and tumorigenesis. -
Herbicide
Chlorimuron-ethyl is a selective herbicide that targets the acetolactate synthase (ALS) enzyme, disrupting branched-chain amino acid biosynthesis in plants. This compound induces oxidative stress, leading to the inhibition of weed growth and development. Chlorimuron-ethyl is primarily utilized in agricultural research, particularly in studies of herbicide resistance and weed management strategies in soybean production. -
Metabolite of The Herbicide Triclopyr
3,5,6-Trichloro-2-pyridinol (TCPy) is a significant metabolite of the herbicide Triclopyr. This compound has been implicated in various biological activities, including associations with attention deficit hyperactivity disorder (ADHD), as well as reductions in testosterone levels. Research indicates that TCPy can induce hearing loss, hepatotoxicity, and nephrotoxicity in murine models, making it a valuable target for investigations related to environmental toxicology and its impacts on human health. -
Protoporphyrinogen Oxidase Inhibitor
Flumioxazin is a selective inhibitor of protoporphyrinogen oxidase, employed primarily in agricultural applications as an herbicide for crops such as soybean and peanut. In addition to its herbicidal activity, Flumioxazin features a reactive alkyne group, allowing it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc). This property makes it a valuable reagent in click chemistry, facilitating the synthesis of various bio-conjugates and enabling the development of innovative chemical probes in research settings. -
Herbicide
Chloramben (3-Amino-2,5-dichlorobenzoic acid) functions as a pre-emergence herbicide targeting a range of annual grasses and broadleaf weeds. It inhibits the growth of weed seedlings, making it a valuable tool in agricultural pest management. Its unique mechanism of action facilitates effective control of unwanted vegetation in various cropping systems. -
Herbicide
Pyroxasulfone is a broad-spectrum pyrazole herbicide that targets residual weed control in crops such as corn and soybeans. It exhibits significant biological activity against a range of annual grasses and certain broadleaf weeds by inhibiting early seedling growth through root and stem absorption. This compound serves as a valuable tool for investigating herbicide impacts and understanding mechanisms of weed resistance in agricultural research. -
Diphenyl Ether Herbicide
Oxyfluorfen is a diphenyl ether herbicide that acts primarily as a protoporphyrinogen oxidase inhibitor, disrupting photosynthesis by interfering with chlorophyll synthesis. It effectively controls a range of annual broad-leaved and grass weeds in both pre- and post-emergence applications. Additionally, Oxyfluorfen has been shown to inhibit cell growth and induce DNA damage. Its ecological impact extends to aquatic species, such as Paramisgurnus dabryanus, where it can cause genome-level detrimental effects, including stunted skeletal growth and limb abnormalities. -
Herbicide
Butachlor is an acetanilide herbicide that primarily targets photosynthetic processes in plants, leading to inhibition of growth. It demonstrates significant chronic toxicity to microalgae and acute toxicity to aquatic organisms, highlighting its potential environmental impact. Additionally, studies have shown that Butachlor adversely affects the reproductive success of zebrafish, making it relevant for research in ecotoxicology and environmental science. -
Herbicide
Pyraflufen-ethyl is a phenylpyrazole herbicide that targets protoporphyrinogen oxidase (PPO), effectively managing annual and perennial broadleaf weeds. This compound demonstrates potent activity against specific species, including the rosette of Parthenium hysterophorus. Pyraflufen-ethyl is valuable in agricultural research and herbicide efficacy studies, particularly in the context of weed management strategies. -
Herbicide
Mecoprop is a selective herbicide that primarily targets the growth of dicotyledonous weeds. It functions by inhibiting auxin transport and disrupting hormonal balance, leading to uncontrolled plant growth and eventual death. Mecoprop is commonly employed in agricultural research to investigate herbicide resistance mechanisms and to develop strategies for effective weed management in various crops. -
Herbicide
Cyanazine is a triazine herbicide targeting multiple species of grass and broadleaf weeds. It exhibits effective herbicidal activity, making it suitable for use in agricultural practices aimed at weed management. Additionally, studies indicate that cyanazine is non-genotoxic, supporting its safety profile for applications in chemical research. -
Herbicide
Clomazone is a systemic herbicide that acts by inhibiting carotenoid biosynthesis. This mechanism leads to the development of albinism in treated plants, resulting from chloroplast membrane disruptions and subsequent chlorophyll degradation. It effectively controls a range of annual broadleaf and grass weeds in crops such as rice, soybeans, and peanuts. Additionally, Clomazone has been shown to exhibit toxic effects on non-target organisms, causing issues like aquatic lethality, developmental malformations, liver damage, mitochondrial dysfunction, and hematotoxicity, making its ecological impact an important consideration in agricultural practices. -
Imidazolinone Herbicide
Imazethapyr is an imidazolinone herbicide that selectively inhibits the acetolactate synthase (ALS) enzyme, crucial for the synthesis of branched-chain amino acids in plants. This compound provides effective control of a wide range of broadleaf weeds and annual grasses, promoting healthy crop growth. Imazethapyr is widely utilized in agricultural research to study herbicide resistance and weed management strategies. -
Preemergence Herbicide
Triallate is a selective preemergence herbicide that targets the control of wild oats in barley, wheat (including spring, Durum, and winter), and sugar beets. Its mechanism involves the inhibition of fatty acid elongation and surface lipid (wax) biosynthesis, making it effective for managing specific grassy weeds. This compound is utilized in agricultural research to improve crop yield and optimize weed management strategies. -
Herbicide
Anilofos is an organophosphorus herbicide primarily targeting weed growth through its pre-emergence application. It inhibits various biological processes in plants, leading to reduced seed germination and growth. While effective as a herbicide, Anilofos exhibits moderate toxicity in mammals and is primarily used in agricultural research to study herbicidal mechanisms and plant responses. -
Herbicide
Simetryn is a selective herbicide that targets photosynthesis in plants, primarily inhibiting the electron transport chain in photosystem II. It exhibits effective herbicidal activity, demonstrating an IC50 value ranging from 16.9 to 3.70 mg/L (79.3 to 17.4 µM). Simetryn is widely used in agricultural research for developing and evaluating herbicide resistance in various crops and studying the ecological impact of herbicides on non-target species.
